Canonical Allele Identifier: CA470832038
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540314C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780557C>G , CM000672.2:g.94780557C>G GRCh38
NC_000010.10:g.96540314C>G , CM000672.1:g.96540314C>G GRCh37
NC_000010.9:g.96530304C>G NCBI36
NG_008384.2:g.22852C>G
NG_008384.3:g.22877C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.540C>G MANE Select ENSP00000360372.3:p.Ser180=
ENST00000645461.1:n.1593C>G
ENST00000371321.7:c.540C>G ENSP00000360372.3:p.Ser180=
ENST00000464755.1:n.1303C>G ENSP00000483243.1:p.=
NM_000769.2:c.540C>G NP_000760.1:p.Ser180=
NM_000769.4:c.540C>G MANE Select NP_000760.1:p.Ser180=